Canonical Allele Identifier: CA341277706
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1660983760
gnomAD v4: 1-94056626-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94056626A>G , CM000663.2:g.94056626A>G GRCh38
NC_000001.10:g.94522182A>G , CM000663.1:g.94522182A>G GRCh37
NC_000001.9:g.94294770A>G NCBI36
NG_009073.1:g.69524T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2357T>C MANE Select ENSP00000359245.3:p.Met786Thr
ENST00000649773.1:c.2161-1311T>C ENSP00000496882.1:n.2161-1311T>C
ENST00000370225.3:c.2357T>C ENSP00000359245.3:p.Met786Thr
ENST00000536513.5:c.-65+6548T>C ENSP00000439707.2:n.-65+6548T>C
NM_000350.2:c.2357T>C NP_000341.2:p.Met786Thr
NM_000350.3:c.2357T>C MANE Select NP_000341.2:p.Met786Thr